Variant #0001041661 (NC_000017.10:g.17700005_17700010del, NM_030665.3:c.3743_3748del (RAI1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17700005_17700010del
DNA change (hg38) -
Published as RAI1(NM_030665.3):c.3743_3748delGCAGCA (p.S1248_S1249del), RAI1(NM_030665.4):c.3743_3748del (p.(Ser1248_Ser1249del))
ISCN -
DB-ID RAI1_000174 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SREBF1 NM_004176.4 -/. - c.*15938_*15943del r.(=) p.(=)
RAI1 NM_030665.3 -/. - c.3743_3748del r.(?) p.(Ser1248_Ser1249del)


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